Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

4 matching diseasesClear search ×

Porphyria due to ALA dehydratase deficiency

ALAD porphyria · Porphyria due to ALAD deficiency

ORPHA:100924

Hepatic porphyria

ORPHA:659694

Porphyria

ORPHA:738

Variegate porphyria

Protoporphyrinogen oxidase deficiency · Porphyria variegata

ORPHA:79473